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CD180-negative B cells play a crucial role in the development of SLE-like morbidity in NZBWF1 mice.

https://repo.qst.go.jp/records/70718
https://repo.qst.go.jp/records/70718
6d4926f9-dbb7-4246-b45d-bd75581bb5ae
Item type 会議発表用資料 / Presentation(1)
公開日 2012-03-22
タイトル
タイトル CD180-negative B cells play a crucial role in the development of SLE-like morbidity in NZBWF1 mice.
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference object
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Fujita, Kazuko

× Fujita, Kazuko

WEKO 694643

Fujita, Kazuko

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Kuwabara, Taku

× Kuwabara, Taku

WEKO 694644

Kuwabara, Taku

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Bing, Wang

× Bing, Wang

WEKO 694645

Bing, Wang

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Tanaka, Kaoru

× Tanaka, Kaoru

WEKO 694646

Tanaka, Kaoru

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Kamata, Itaru

× Kamata, Itaru

WEKO 694647

Kamata, Itaru

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Akasaka, Yoshikiyo

× Akasaka, Yoshikiyo

WEKO 694648

Akasaka, Yoshikiyo

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Ishii, Toshiharu

× Ishii, Toshiharu

WEKO 694649

Ishii, Toshiharu

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藤田 和子

× 藤田 和子

WEKO 694650

en 藤田 和子

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桑原 卓

× 桑原 卓

WEKO 694651

en 桑原 卓

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王 冰

× 王 冰

WEKO 694652

en 王 冰

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田中 薫

× 田中 薫

WEKO 694653

en 田中 薫

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抄録
内容記述タイプ Abstract
内容記述 Systemic lupus erythematosus (SLE) is a disease usually caused by aberrant self-tolerance, in which self-reactive T and B cells are activated, resulting in production of various autoimmune antibodies. A recent study demonstrated that TLRs appear to play a role in the production of autoimmune antibodies. CD180 is a homologue of TLR 4 and a key regulator of proliferation and cell death expressing on B lymphocyte. In SLE patients, the population of CD180-negative B cells in the peripheral blood is significantly increased and changes in parallel with SLE disease activity. In the present study using NZBWF1 mice, we explored the role of CD180-negative B cells in the development of systemic autoimmune disorders and in the pathogenesis of lupus-like nephritis. The results showed that the population of CD180-negative B cells in spleen increased with age and well correlated with grades of renal lesions. In addition, CD180-negative B cells obtained from the spleen produced anti-dsDNA antibody in vitro. The amount of the antibody in peripheral blood of the mouse remarkably increased with advancing age. These results indicated that the CD180-negative B cells significantly participate in the progression of SLE-like morbid condition. In further experiments, infiltrated B cells into the renal lesion were characterized to be CD180-negative and proved to produce anti-dsDNA antibody in vitro. In conclusion, the present study revealed that CD180-negative B cells play a crucial role in the development of SLE-like morbidity in experimental NZBWF1 mice.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 第40回日本免疫学会学術集会
発表年月日
日付 2011-11-29
日付タイプ Issued
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